Aquatic Macroinvertebrate Inventory & Assessment of
Springs and Seeps within Bighorn Canyon National
Recreation Area (BICA)
Prepared for the:
Western National Parks Association and the Greater Yellowstone Network
Inventory & Monitoring Program, National Park Service
Layout Creek Spring looking downstream
By:
David M. Stagliano
Aquatic Ecologist
March 2008
i MONTANA
Natural Heritage
Program
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Aquatic Invertebrate Surveys of BICA Seeps and Springs
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Stagliano
Table of Contents
Introduction 3
Methods 4
Macroinvertebrate Collection 4
Macroinvertebrate Analysis 5
Spring Habitat Classification 5
Results 6
Spring Habitat Evaluation 6
Macroinvertebrate Communities 9
Discussion 12
Conclusions and Recommendations 13
Literature Cited 14
Appendix A. Macroinvertebrate Species List for all BICA samples.
Acknowledgements
Financial support for this survey and analysis was provided by a grant from the Western National
Parks Association facilitated by Elizabeth Crowe and Brenda Acker, Research Coordinator. We
especially want to thank Denine Schmitz for logistical support, field assistance, maps, water-quality
data and sampling permit assistance, we could not have accomplished so much without her help.
We would like to thank Cass Bromley, the BICA ecologist for logistical support, and Darrell Cook,
BICA park superintendent for his endorsement to allow us to proceed with this project. I
additionally want to thank Dr. Robert Wisseman and Brady Richards (taxonomic guru's) who
verified beetle and caddisfly identifications. Fieldwork was assisted by Linda Vance (MTNHP).
All photos in the report were taken by MTNHP personnel, unless otherwise noted
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INTRODUCTION
Spring ecosystems in arid regions are oftentimes the only permanent water source in the uplands
and provide essential habitat for a myriad of aquatic and terrestrial organisms (Erman 2002); they
are essentially aquatic islands in a sea of desert (Thompson et al 2002). Riparian areas adjacent to
springs can provide habitat to up to 75% of the available species diversity in arid regions (Shepard
1993). Spring ecosystems have evolved within a narrow set of environmental conditions strictly
dependent on groundwater discharge (Shepard 1993). Discharge of springs within Bighorn
Canyon National Recreation Area (BICA) has been found to be dependent on snowmelt-based
groundwater reaching outflows as recently as weeks after melting, to as long as years after (D.
Schmitz, pers. comm.). The mosaic of microhabitats in springs is largely due to stable, long-term
flow rates (Perla & Stevens 2003), and perennial discharge has been linked to diverse, unique and
often endemic flora and fauna (Myers 1995, Sada and Vinyard 2002). Aquatic macroinvertebrates
can make up a substantial proportion of spring biodiversity. Aquatic species in spring ecosystems
can display a high degree of endemism, often evolving to subtle cues in water chemistry (Arsufi
1993, Heino et al. 2003; Sada et al. 2005). Macroinvertebrate populations in springs of the Great
Basin, Sierra Nevada, and Colorado Plateau are known to support endemic aquatic
macroinvertebrates (Erman 2002; Hershler and Sada 2002; Sada and Herbst 2001). An initial
survey of Great Basin Springs reported four new species of aquatic invertebrates (Myers 1995). A
new species of the springsnail, Pyrgalopsis (the only species reported east of the continental
divide) has recently been found in a Missouri River (Montana) spring (Hershler and Gustafson
2002). Even though most spring locations in BICA have been documented on USGS topographic
maps, there has been no documentation of aquatic fauna occurring within these ecosystems.
Figure 1. Overview location of Bighorn Canyon National
Recreation Area (reprinted from Baum and Peterson 2001).
^1
YrtllnwljiHOim
Spring flora and fauna in BICA
have only been investigated for the
occurrence of rare riparian and
wetland plants (ex. Sullivantia
hapemanii var. hapemanii) (Heidel
and Fertig 2000).
Therefore, a survey of spring fauna
will substantially increase the
known BICA species and document
potentially rare, endemic or
endangered species. Surveys in this
area will fill data gaps, serve as a
reference point for change
detection, provide a baseline
necessary for evaluating the rarity
of different spring ecosystem types,
and form an understanding of
biological diversity and integrity at the local and ecoregional level. Many spring species have
narrow environmental ranges (specialists) and therefore are susceptible to changes in water
chemistry and habitat quality.
Our main objectives for this study include 1) an initial aquatic invertebrate faunal survey and
bioassessment of targeted perennial BICA springs, 2) determining the environmental factors that
determine biointegrity of the aquatic macroinvertebrate communities spring ecosystem, and 3)
•i r-i- !■ ni L«nd«
USPS NATIONAL FOREST
BIGHORN CANYON NATIONAL RECREATED AREA
| USFS ESTABLISHED WILDERNESS AREA
| YELLQWIAJL WILDl IFE HABITAT MANAGEMENT AREA
CROA'ihDljWjRFSefiWATON
31 March 2008
Aquatic Invertebrate Surveys of BICA Seeps and Springs
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Stagliano
provide a sampling scheme and identify indicator measures (species richness, abundance, target
species (i.e. endemics), etc.) with which to monitor spring diversity and biointegrity in the future.
Achieving our objectives, especially the third, will allow park managers to monitor the status and
changes of aquatic macroinvertebrate indicators over time within BICA springs. This process can
be repeated every five years for any proposed spring-type monitoring protocol: an impaired (cattle
or human impacted) sample and a reference (pristine) condition sample from each spring type.
Macroinvertebrate Collection & Analysis
We collected macroinvertebrate samples and habitat data May 19-22, 2007 from 21 priority BICA
spring & seep sites (D. Schmitz, pers. comm.). Protocols dictated sampling for macroinvertebrates
within 100m of origination of the spring, and this distance was usually much shorter (~0-25m from
the orifice), especially for wall seeps.
Additionally, we collected samples from the
run-out channels of 5 springs where changing
water & habitat conditions can lead to different
invertebrate assemblages (Bear Spring, Layout
Creek, Picket's Wall and Lockhart
Springhouse { 2 } ) . Sampling methodology was
site-specific, and largely dependent on the
length and magnitude of the spring flow.
Semi-quantitative field sampling protocols
employed a minimum of 10 randomized 0.5m
jabs or kicks allocated to all habitats within a
spring reach using a standard 500 micron D-
frame net or in shallow, low flow situations, an
aquarium net. All substrates were disturbed and washed into the net (Photo 1, taken by D. Sasse).
The contents of the ten individual samples were placed in a 40L bucket, washed and elutriated
allowing mineral matter to remain on the bottom of the bucket, while inverts and organic materials
are collected onto a 500 micron sieve, and placed in a 1L Nalgene container filled with 95%
Ethanol (ETOH) for preservation. The mineral portion on the bottom of the bucket was scanned for
caddisfly cases, snail or clam shells before returning it to the spring. For spring reaches at least
40m long and at least 10cm in depth a
Table 1. Impairment determinations from MMI and O/E
(RIVPACS) models (from Jessup 2005, Feldman 2006).
Ecoregion
Mountain
Low Valley
Eastern Plains
RIVPACS
>0.8 or < 1.2
<0.8 or > 1.2
>0.8 or < 1.2
<0.8 or > 1.2
>0.8 or < 1.2
<0.8 or > 1.2
>63
<63
>48
<48
>37
<37
Impairment Determination
Not impaired
Impaired
Not impaired
Impaired
Not impaired
Impaired
reach- wide composite type sample
(EMAP reach- wide 10 transect protocol,
Lazorchak et al. 1998) was used. Since
EMAP protocols call for equal spacing of
samples in the reach, this sampling can
be more easily replicated for monitoring
capabilities. The samples were processed
(sorting, identification, and data analysis)
by the author in Helena following MT
Department of Environmental Quality's
protocols (MT DEQ 2005).
Macroinvertebrates were enumerated & identified to the lowest taxonomic level using a 4-40x
Stereo-zoom Microscope, imported into an Access-based ED AS database, and multimetric
macroinvertebrate (MMI) metrics were calculated from the data (Jessup et al. 2005, Feldman
2006). Metric results were then scored using the MT DEQ criteria and each sample categorized as
31 March 2008
Aquatic Invertebrate Surveys of BICA Seeps and Springs
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non-impaired or impaired according to specific threshold values (Table 1). Most BICA spring sites
are categorized as Low Mountain/Valley (LVAL) and rated accordingly, although we did run an
alternate MMI, as mountain or prairie for a QC check. The impairment threshold set by MT DEQ
for the LVAL Index is 48, thus any score above this threshold are considered unimpaired. The
MMI score is based on metrics that measure attributes of benthic macroinvertebrate communities
that change in response to stream condition changes (anthropogenically caused). Expected
reference condition indicator species for perennial spring macroinvertebrate communities were
derived from springs in the Northwestern Great Plains (NWGP)(Stagliano et al. 2006).
Spring Habitat Classification
The landscape surrounding the springs of the BICA is typical of the Pryor-Big Horn Foothills /
Wyoming Basin ecoregion (Woods et al. 2002). Twenty-one springs identified as Wyoming Basin
Perennial Spring Aquatic Ecological System Types (AES S005) were visited (Figure 2). All
springs are initially classified into 2 types: Limnocrenes — non-linear flowing springs, lentic spring
ecosystems that resemble small wetlands (WPSS-Wetland /Ponded Seep Springs), and
Rheocrenes - flowing water springs that may flow into perennial or ephemeral streams or may
disappear into the ground some distance from their source (Table 2 & 3). Headgate Seep and
Pentagon Spring were included into the WPPS classification because of their wetland seepage
characteristics, but had some degree of directional flow. Secondarily, Rheocrenes can be separated
into dispersed wall spring seeps, a.k.a. hanging gardens (LVWS-Low, MVWS-Med or High
Volume Wall Springs & Seeps) or linear flowing channelized springs (STCS-Single Thread
Channel Springs) (Figure 2, Table 2). A rare form of hanging garden within BICA is the Karst
wall rheocrene (photo left). Karst hanging gardens are
assemblages of aquatic and semi-aquatic plants, including
the sensitive Sullivantia hapemanii, and animals occurring
at seeps on calcareous (limestone) canyon walls.
Spring Habitat Evaluations. Overall, 6 of the 2 1
spring sites ranked good-excellent and 8 had fair habitat
quality assessed by EPA's field RBP protocols (Table 2).
Five sites were ranked slightly impaired, and 2 moderately
to severely impaired. Highest site habitat scores were
MVWS, LVWS wall seeps and STCS increasing in distance
from previously occupied areas. Highest deductions to the
riparian assessment scores were in-stream sediment, bare
ground and bank trampling by cattle intrusions into the
riparian zone. These intrusions were specifically noticeable
and had very high impacts at North Davis and Lockhart
Stockpond Springs. Human impacts on springs at historic
ranches (intended or inadvertent) have resulted in many of
the impairments seen at BICA springs, including the occurrence of non-native species. Rorippa
nasturtium (watercress) is an obvious example of an introduced plant species occurring at 9 of 21
spring sites (personal observation), most of these sites are within the Hillsboro, Lockhart or Ewing-
Snell Ranch areas or are adjacent to roadways.
Pickett's Wall, a Karst wall rheocrene
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Aquatic Invertebrate Surveys of BICA Seeps and Springs
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Table 2. Spring Station information. Spring classes (LVWS, MVWS, STCS, WPSS) are assigned and
described in the text. HHR=Habitat Health rank by riparian/stream evaluations (++) good-excellent,
(+) fair-good, (-) poor, (--) degraded. C=conductivity in us/sec, T=temp °C, Q=flow in liters/sec.
Station ID
Station Name
SPR#
Spring
Class
UTM83
X
UTM83
Y
HHR
PH
C
Temp
Q
L/s
B_BEARSPR_run
Bear Spring run
22
WPSS
717270
5002620
+
7.12
na
14.0
na
B_BEARSPR1
Bear Spring
22
WPSS
717270
5002620
-
7.10
na
12.0
na
B_CASS_SPR1
Cass Spring
33
STCS
716094
4999499
++
7.14
182
10.0
6.800
B_CATTRKSPR1
Cattrack Spring
13
STCS
717230
4998805
+
7.11
2004
11.3
0.078
B_FINLEYSPR1
Finley Spring nr
29
STCS
45.1158
108.2106
++
6.97
1867
10.8
0.215
B_HDGTSEEP1
Barry s Landing
Headgate Seep
24
WPSS
713576
4996931
+
7.27
399
13.1
na
B_HIDDENSPR1
Hidden Spring
STCS
718192
4998344
++
6.88
1367
11.6
9.000
B_HLSBMNSPR1
Hillsboro Main
7
MVWS
717144
4997926
++
7.20
578
10.2
9.883
B_HLSBSDSPR2
Spring
Hillsboro Side
6
LVWS
717230
4997814
+
7.48
479
9.9
0.027
B_LAYOUTSPRl
Spring2
Layout Spring
4
MVWS
712782
4997451
++
7.74
316
5.4
6.097
B_LAYOUT_dn
Layout Bottom
4
MVWS
712782
4997451
++
7.74
316
8.0
6.097
B_LCKHOSSPRl
Lockhart
19
STCS
716942
5001986
.
6.98
1260
10.0
0.308
B_LCKHOS_Run
Springhouse
Lockhart Spring
19
STCS
716942
5001986
+
6.98
1260
12.0
0.308
B_LCKHOS_Run2
run
Lockhart spring
run2
19
STCS
716942
5001986
+
6.98
1260
13.0
0.308
B_LCKSOSPRl
Lockhart South
18
STCS
716744
5001901
+
6.88
1445
10.0
0.008
B_LOCKPNDSPl
Spring
Lockhart
17
WPSS
716456
5001682
7.18
2383
10.7
0.040
B_MASLOVSPRl
Stockpond
Mason-Lovell
1
WPSS
724616
4967924
6.88
1514
15.5
0.013
B_NDAVISPR1
Spring
N Davis Spring
21
STCS
716466
5002406
_ _
7.13
1746
10.3
0.015
B_PENTAGSPR1
Pentagon Spring
15
WPSS
714074
4998991
-
6.77
433
8.8
na
B_PICKETSPR1
Pickett's Wall
10
LVWS
717541
4998619
+
6.89
875
8.7
na
B_PICKETS_run
Seep
Pickett's Wall_
runout
10
LVWS
717541
4998619
+
7.20
875
12.0
na
B_RICKSSPR1
Rick's Spring
20
STCS
716910
5002153
+
6.66
1195
11.5
0.150
B_SORENSPRl
Sorenson spring
3
STCS
715222
4995906
-
7.58
427
9.4
4.410
B_TRCPGDSPR1
Trail Creek CG-
Main
27
MVWS
718131
4998500
++
6.86
1844
10.8
0.660
B_TRCPGDSPR2
Trail Creek CG
2
Tyler's Torrent
28
LVWS
718131
4998517
+
6.72
1286
9.5
0.230
B_TYLTORSPRl
8
STCS
717473
4998020
+
6.94
1105
9.4
0.238
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Aquatic Invertebrate Surveys of BICA Seeps and Springs
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Figure 2. Location (A), classification (B) and biointegrity (C) of sampled BICA springs with magnification of MT spring sites; only one
spring was sampled in WY (Mason-Lovell, Spr #l-white circle). Spring number, biointegrity rankings and class types (LVWS, MVWS,
STCS, WPSS) are assigned and described in the text and in Table 3.
<\ Seeps and Springs
Stagliano
Table 3. Spring Habitat Types with representatives of differing ecological integrity classes.
BICA Spring
Classification
High Quality Ecological
Condition
Moderate Ecological
Condition
Impaired Ecological
Condition
Rheocrenes - directional flowing water springs & seeps that may flow into perennial or ephemeral streams.
1) Single Thread
Channel Springs
(STCS)
2) Low Volume
Wall Springs &
Seeps (LVWS)
3) Med-High
Volume Wall
Springs &
Seeps (MVWS)
Cass, Finley Spring (photo),
Lockhart Spring Run
Cattrack, Hidden, Rick's (photo),
Sorenson, Tyler's Torrent Spring
jBf'AkjL.
North Davis (photo),
Lockhart South Spring
Lockhart Springhouse
No representative of an
impaired wall spring
Pickett's Wall Spring
Trail Creek Camp #2 Spring
(Above), Hillsboro Side Spring
No representative of an
impaired wall spring
Layout Spring (above), Hillsboro
Main Spring
Trail Creek Campground Main
Spring
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Table 3 (cont).
Non-Impaired
Slightly-Impaired
Impaired
BICA Spring
Classification
Limnocrenes - non-linear flowing spring water, lentic spring ecosystems that resemble small wetlands
1) Wetland /Ponded
Seep Springs
(WPSS)
Headgate Seep Spring
Bear (above) & Pentagon
Spring
Mason-Lovell Spring
2) Artificially
Created Wetland /
Ponded Springs
(WPSS)
No representative of an
un-impaired ponded
spring
KM
■ an
Sorenson Spring Pond Lockhart Stockpond
Aquatic Macroinvertebrate Community Results
Overall, 146 macroinvertebrate taxa were identified from 21 springs (26 samples) within the 4
habitat types. Diptera (true flies) were the richest order with 69 taxa, followed by Trichoptera
(caddisflies) and Coleoptera (beetles) with 19 taxa apiece (Appendix A). The most diverse site was
Layout Spring with 33 total taxa, and the most diverse spring class type is the Med-High Volume
Wall Spring (n=4) averaging 27 taxa per sample. Low Volume Wall Springs (n=4) and Single
Thread Channel Springs (n=l 1) had similar avg. richness at -20 taxa, while Wetland Seep Springs
(n=7) had significantly lower richness averaging -13 taxa. Twenty-four of the 26 samples were
processed completely (every invertebrate was picked), and in 20 of those cases, the minimum
number of organisms was still not reached (only 2 had to sub- sampled).
No species of concern, threatened or endangered invertebrate species were collected during the
surveys. Two introduced species were reported, the wide-ranging amphipod, Hyalella azteca
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(Sorenson Spring), and the snail, Pseudosuccinea columella (Hidden, Pickett's & Sorenson Springs).
A number of cold-water, habitat-restricted, sensitive taxa (14 spp.) were found only at Layout Creek
spring (see table), with a few of those taxa found additionally at Hidden, Rick's, Pickett's Wall, Trail
Creek Campground Main and the runout of Lockhart Springs. Four free-living, predatory
caddisflies: Rhyacophila verrula (photo 3), R. oreta, R. brunnea gr. & R. rotunda were only found
together at Layout Spring (Inset Table).
• Ecologically-important spring indicator taxa
(Stagliano 2006), the stonefly-
Amphinemura banksi, the riffle beetle -
Optioservus quadrimaculatus and the
ma.yf\y-Baetis tricaudatus were reported
from 16 BICA spring sites, the tipulids
Dicranota and Tipula at 10 sites, the
diptera, Caloparyphus (7), the beetle,
Hydroporus (7), and the caddisfly,
Hesperophylax designatus at 6 sites (Table
3). Indicator taxa of ecologically "healthy"
springs at BICA, that were not reported
from NWGP springs, were the
Chironomidae Brillia; the riffle beetle,
Heterlimnius corpulentus; caddisfly-
Lepidostoma unicolor; and predatory
stonefly; Hesperoperla pacifica (photo 4)
found at 16, 14, 12 & 13 sites, respectively
(Table 3, Appendix I).
• Total taxa richness at a site was not a good
overall indicator of biointegrity. For
example Bear Spring run, Cattrack and
Finley's had low richness for a STCS (13-
15 taxa), but still reported good ecological
rankings. Conversely, Lockhart Stockpond,
Mason-Lovell and N. Davis Springs had 17
taxa, but were ecologically impaired.
Unique "Cool" Taxon
Layout
Other
Creek
BICA
Sites
Stoneflies
Malenka sp.
+
Paraperla cf. frontalis
+
Sweltsa sp.
+
Zapada oregonensis
+
Mayflies
+
Ameletus similior
Baetis bicaudatus
+
Caddisflies
Rhyacophila verrula
+
Rhyacophila oreta
+
+(3)
Rhyacophila brunnea gr.
+
+(1)
Rhyacophila rotunda
+
-
Homophylax
+
-
Neothremma alicia
+
-
True Flies
Boreochlus persimilis
-
+
Cardiocladius
+
+(2)
Paraphaenocladius
+
+(2)
Pagastia
+
-
Diplocladius
+
-
Eukiefferiella brehmi gr.
+
+(2)
E. devonica gr.
+
-
E. pseudomontana gr.
+
-
Krenosmittia
+
+(1)
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Table 3. Indicator taxa of good to excellent
ecological integrity in NWGP and BICA rheocrene
perennial springs. (++) = highly significant indicator,
(+) = significant, (-) = not significant or not found in
spring ecosystem.
Indicator Taxon
NWGP
BICA
Stoneflies
Amphinemura banksi
Hesperoperla pacifica
Mayfly
Baetis tricaudatus
Caddisflies
Hesperophylax cf. designatus
++
++
++
++
++
++
+
Lepidostoma unicolor
-
++
Damselfly
Argia
Beetles
Optioservus
Heterlimnius corpulentus
Hydroporus
Oreodytes
Diptera (True Flies)
Brillia
Caloparyphus
Dicranota
Dixa
Euparyphus
Heleniella
Odontomesa
Ormosia
Pedicia
Parametriocnemus
Pseudodiamesa
Radotanypus
Tvetenia bavarica Gr.
Tipula
++
+
+
+
+
+
+
+
+
+
+
+
++
++
+
++
+
+
+
+
+
++
++
+
Results from the habitat and macroinvertebrate
• Lower taxa richness was recorded directly at the
spring orifice than in samples taken just a few
meters downstream (Pickett' s Wall, Trail Creek
Campground Main), and this is especially true of
modified springs (ex. Sorenson's, Lockhart
Springhouse). In addition, the runouts from
spring origins acquired additional taxa along an
increasing temperature and habitat gradient.
^Example: Bear Spring's (a slightly-impaired
WPSS) runout just 20m from the source gained
enough rheocrene indicator taxa to classify as
a non-impaired STCS (Table 4).
• Using MT DEQ's MMI, 15 of the 26 spring
samples sites were ranked non-impaired (good to
excellent biological integrity), 8 were slightly
impaired and 3 was severely impaired (Table 4).
There were numerous discrepancies between
biological community scores & ecological health.
^Example 1: Mason-Lovell is a silted, impaired
WPSS with low numbers of macroinvertebrates,
but ranked high with both MMI evaluations.
^Example 2: Hidden Spring is in good
ecological health, has high taxa richness
and # of BICA indicator species, but ranked
severely impaired by both MMI evaluations.
• Pickett' s Wall run and Layout Creek Spring
were the only samples to be ranked similarly by
all integrity measures. Without considering the
alternative MMI and NWGP taxa (Table 4), the
sites with the highest ranking agreements are:
Bear_run, Cass, Headgate, Hillsboro Main and
Side Springs, Layout (both), Trail Creek
Campground Main and #2 Springs,
surveys combined to rank the following sites:
Overall BICA Perennial Spring Aquatic Ecological System Condition and Biological Integrity (in
order of highest integrity to worst by spring class type):
1) Med-High Volume Wall Springs (MVWS)-l) Layout Creek, 2) Trail Creek Campground
Main and 3) Hillsboro Main Spring.
2) Low Volume Wall Springs (LVWS)-l) Pickett's Wall Spring + run, 2) Trail Creek
Campground #2, 3) Hillsboro Side Spring.
3) Single Thread Channel Springs (STCS)- 1) Cass, 2) Finley 3) Rick's 4) Lockhart
Spring Run, 5) Hidden, 6) Cattrack 7) Sorenson, 8) Tyler's Torrent, 9) Lockhart South
10) Lockhart Springhouse, 11) North Davis Spring
4) Wetland / Ponded Springs (WPSS)-l) Headgate Seep, 2) Bear, 3) Pentagon 4) Mason-
Lovell Spring, 5) Lockhart Pond Spring
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Aquatic Invertebrate Surveys of BICA Seeps and Springs
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Table 4. Aquatic integrity ranking of all inventoried sites. Total number of invertebrates, total taxa
richness (T_Taxa), LVAL and Alternative (MTN or Plains) MMI scores and expected aquatic
communities assessed against similarly classified reference sites (Observed/ Expected). (++) = high
biological integrity, (+) = good integrity, (-) = slightly impaired, (--) = moderate to severely impaired
biological community. Shaded-cells represent good to excellent scores above set thresholds.
StationID
Spr
#
Total
Ind.
T Taxa
LVAL
MMI
Score
MMI
Rank
Alt.
MMI
Score
Alt.
MMI
Rank
#
NWGP
spring
taxa
% ref.
spring
taxa
#
BICA
ID
taxa
%
BICA
spring
taxa
B_BEARSPR_run
B_BEARSPR1 (L)
B_CASS_SPR1
B_CATTRKSPR1
B_FINLEYSPR1
B_HDGTSEEP1(L)
BJHIDDENSPR1
BJHLSBMNSPR1
BJHLSBSDSPR2
B_LAYOUT_LOW
BJ.AYOUTSPR1
B_LCKHOS_Run
B_LCKHOS_Run2
BJ.CKHOSSPR1
BJ.CKSOSPR1
BJ.OCKPNDSP
B_MASLOVSP (L)
B_NDAVISPR
B_PENTAGSP (L)
B_PICKETS_run
B_PICKETSPR1
B_RICKSSPR1
B_SORENSPR1
B_TRCPGDSPR1
B_TRCPGDSPR2
B TYLTORSPR1
22
22
33
13
29
24
7
6
4
4
19
19
19
18
17
1
21
15
10
10
20
3
27
28
8
106
64
186
183
175
386
80
123
210
154
272
150
161
23
297
207
96
106
40
146
31
388
256
261
345
357
13
11
49.8
56.2
+
+
53.9
+
3
3
5
4
5
6
4
5
5
5
6
5
5
3
2
3
3
18.8
18.8
31.3
23.5
31.3
35.3
25.0
31.3
31.3
31.3
37.5
31.3
31.3
0.0
18.8
0.0
11.8
18.8
18.8
7
41.2
31.9
48.6
49.6
40.4
38.3
26.5
48.7
37.9
-
0.0
24
56.9
+
11
64.7
15
15
24
26
24
22
24
33
80.0
57.5
66.3
++
+
++
5
29.4
7
7
7
10
10
8
41.2
41.2
41.2
58.8
58.8
47.1
28.2
—
65.2
49.8
83.0
+
+
++
61.4
63.9
+
++
68.1
+
7
9
9
41.2
52.9
52.9
18
20
6
17
13
17
17
7
19.7
32.6
33.5
19.7
34.5
-
21.9
28.3
4.6
21.7
19.6
--
0.0
10
58.8
1
2
2
2
5.9
11.8
11.8
11.8
76.5
++
69.5
++
49.4
36.4
+
31.1
15.1
-
24
8
47.2
57.2
+
+
53.5
+
7
43.8
10
58.8
35.2
31.1
30.9
46.5
43.2
42.1
-
4
25.0
4
23.5
29
21
27
25
34.8
37.8
-
9
56.3
9
52.9
4
6
6
4
25.0
37.5
37.5
25.0
4
23.5
56.4
51.0
+
14
14
82.4
82.4
17
33.2
-
6
35.3
Discussion
Although we did not discover any new species during our initial BICA spring surveys, the potential
for documenting additional macroinvertebrate taxa in these systems certainly exists. Many of these
aquatic insects can only be taxonomically identified to species with adult male specimens. Thus,
without collecting adults which can be time consuming and labor intensive, we may never know if a
"new species to science" dwells within the spring ecosystems of BICA. It is very likely that
intensive surveys over multiple seasons could conceivably double our 146 aquatic taxa list.
Although in a study that intensively collected invertebrates from 28 springs in the Great Basin, a
total of 141 taxa were documented, 58 of these were caddisfly species (Myers and Resh 2002). We
identified almost 3 times the number of Diptera (true fly) taxa than that study, but only 19 caddisfly
species. Further, faunal responses to environmental gradients tend to be individualistic and taxon-
specific, and since we have identified multiple taxa to the genus-level, species shifts from one spring
to the next would occur without detection. Springs and wetlands in arid landscapes are characterized
31 March 2008
Aquatic Invertebrate Surveys of BICA Seeps and Springs
Page 12 of 18
Stagliano
by isolation and unpredictable colonization events — BICA springs may be in close enough proximity
to mountain stream taxa (Pryors and Bighorns) to allow population connectivity and genetic flow
preventing speciation events. During this study, we have documented important sources of aquatic
biodiversity within this arid recreation area, and sampled those using protocols that are repeatable
and scientifically credible for park resource managers to implement in long-term monitoring
programs. Given limited funding and time, we did not get a chance to analyze water chemistry
parameters and macroinvertebrate community structure. Spring permanence, discharge and
disturbance are the primary diversity drivers in most spring ecosystems, but further discriminant
analysis has indicated even small changes in temperature, conductivity, alkalinity, and elevation
were responsible for further explanation of species composition structure across spring ecosystems
(Myers and Resh 2002). The widest variation of the water chemistry parameters in BICA was
conductivity (182-2343 us/sec), and in some cases this was correlated with low-flow, impacted
ponded areas (Lockhart Pond Spring and Mason-Lovell), but in others, high values were more
related to subsurface geology (Trail Creek Campground Springs). How naturally high levels of ions
in BICA springs effects macroinvertebrate communities is worth further study.
Conclusions & Recommendations
Spring macroinvertebrate diversity and richness in BICA is positively related to discharge (water
flow) and negatively related to anthropogenic factors (spring diversions, orifice manipulations,
stream habitat degradation). Wall springs were least likely to be human-impacted due to there
position in the landscape. Medium-high volume wall springs had the highest macroinvertebrate
diversity and biointegrity, and taxa richness decreased down the gradient with single thread channel
springs, until the lowest diversity was recorded at impaired low flow wetland springs.
• In terms of monitoring BICA spring macroinvertebrate communities: 10 composite dipnet
samples per site often did not collect the minimum number of organisms (300) for the MMI
metrics. Low numbers of macroinvertebrates are known to cause discrepancies with MMI
scores (Feldman, pers. comm). Replicate samples within a spring reach could be added to
obtain more organisms, but this will increase field and lab processing time and costs.
• The DEQ Low Mountain/Valley MMI performed fairly well at determining biological
integrity of rheocrenes, although limnocrene spring-types and low invertebrate numbers in
the samples seemed to affect it's detection capabilities significantly (Mason-Lovell & Bear
Spring were over-ranked, while Lockhart South and Hidden Spring were under-ranked).
• Expected reference condition indicator species for spring macroinvertebrate communities
that were derived from springs in the Northwestern Great Plains (NWGP) did not perform
well in distinguishing ecological integrity of BICA springs, therefore, we derived a new set
of indicator species reflecting reference condition rheocrene spring conditions.
• Good to excellent macroinvertebrate community integrity of rheocrene springs had at least 7
of the 17 BICA Indicator Species present, and usually more than 20 total taxa. For
limnocrene (WPSS) biointegrity, the LVAL MMI usually over-valued their condition.
• Significant anthropogenic factors (i.e. water diversions, improper grazing practices) still exist
and historic or current agricultural activities (e.g. Lockhart, Ewing-Snell Ranches) are
continuing to threaten biological integrity of numerous springs in BICA. The easiest
recommendation to make is to maintain adequate cattle fencing around these sensitive
riparian spring areas. Springs undergoing riparian protection measures (i.e. fencing,
revegetation) can be monitored for water and biological quality improvements on a yearly or
multiple-year basis, until habitat quality and biointegrity trends start to improve.
31 March 2008 Aquatic Invertebrate Surveys of BICA Seeps and Springs Stagliano
Page 13 of 18
REFERENCES
Arsuffi, Thomas L. 1993. Status of the Comal Springs Riffle Beetle (Heterelmis comalensis), Peck's Cave
Amphipod (Stygobromus pecki Holsinger), and the Comal Springs Dryopid Beetle (Stygoparnus
comalensis Barr and Spangler). Prepared for the U.S. Fish and Wildlife Service.
Erman NA. 1998. Invertebrate richness and trichoptera phenology in Sierra Nevada (California,USA) cold
springs: Sources of variation. Studies in crenobiology: The biology of springs and springbrooks.
Netherlands: Backhuys. p 95-108.
Erman NA. 2002. Lessons from a long-term study of springs and spring invertebrates (Sierra Nevada,
California, USA) and implications for conservation and management. In: Sada DW,Sharpe SE,
editors; 2002; Las Vegas, NV.
Feldman, D. 2006. Interpretation of New Macroinvertebrate Models by WQPB. Draft Report. Montana
Department of Environmental Quality, Planning Prevention and Assistance Division, Water Quality
Planning Bureau, WQS Section Helena, MT 59620. 14 pp.
Heidel, B and W. Fertig. 2000. Rare plants of Bighorn Canyon National Recreation Area. Report to National
Fish and Wildlife Foundation and Bighorn Canyon National Recreation Area. Montana Natural
Heritage Program, Helena, and Wyoming Natural Diversity Database, Laramie. 66 p.
Heino J, Muotka T, Mykra H, Paavola R, Hamalainen H, Koskenniemi E. 2003. Defining macroinvertebrate
assemblage types of headwater springs: implications for bioassessment and conservation. Ecological
Applications 13:842-852.
Hershler R and Sada DW. 2002. Biogeography of Great Basin aquatic snails of the genus Pyrgulopsis.
Smithsonian Contributions to the Earth Sciences 33:255-276.
MTDEQ. 2005. Sample Collection, Sorting, and Taxonomic Identification of Benthic Macroinvertebrates.
Montana Department of Environmental Quality Water Quality Planning Bureau Standard Operating
Procedure WQPBWQM-009. April 2005.
Myers, M. 1995. Aquatic Insects in the Springs of the Great Basin. Department of Environmental Science,
Policy and Management, UC Berkeley.
Myers, M and V. Resh 2002. Trichoptera and other macroinvertebrates in springs of the Great Basin: Species
composition, richness, and distribution. Western N. Am. Nat. Vol. 62, no. 1, pp. 1-13.
Perla B, Stevens LE. 2003. Biodiversity and productivity as an undisturbed spring in comparison with
adjacent grazed riparian and upland habitats. In: Stevens LE, Meretsky VJ, editors. Every last drop:
Ecology and conservation of springs ecosystems. Flagstaff, AZ: University of Arizona Press, p in
press.
Sada DW, Fleishman E, Murphy DD. 2005. Associations among spring-dependent aquatic assemblages and
environmental and land use gradients in a Mojave Desert mountain range. Diversity and
Distrubutions 11:91-99.
Sada DW, Vinyard GL. 2002. Anthropogenic changes in biogeography of Great Basin aquatic biota.
Smithsonian Contributions to the Earth Sciences 33:277-293.
Sada DW, Williams JE, Silvey JC, Halford A, Ramakka J, Summers P, Lewis L. 2001. A guide to managing,
restoring, and conserving springs in the Western United States. Denver: Bureau of Land Mangement.
Report nr 1737-17. 70 p.
Shepard WD. 1993. Desert springs-both rare and endangered. Aquatic Conservation: Marine and Freshwater
Ecosystems 3(4):351-359.
Stagliano, D.M., B.A. Maxell, and S.A. Mincemoyer. 2006. A Multi-Discipline Integrative
Assessment of Lotic Spring Sites in the Custer National Forest (Ashland Ranger District)
http://nhp.nris.state.mt.us/Reports/Custer_Forest_Project_2006.pdf
Thompson B.C., Matusik-Rowan P.L., Boykin K.G. 2002. Prioritizing conservation potential of arid-land
montane natural springs and associated riparian areas. Journal of Arid Environments 50(4):527-547.
Woods, A.J., Omernik, J.M., Nesser, J.A., Shelden, J., Comstock, J.A., Azevedo,
S.H., 2002, Ecoregions of Montana, 2nd edition.
31 March 2008 Aquatic Invertebrate Surveys of BICA Seeps and Springs Stagliano
Page 14 of 18
Appendix A. Macroinvertebrate Species List for all BICA samples. Number of samples the taxon
occurred (# of S) and the Frequency of Occurrence (F of O). Grey Shaded =Rheocrene Indicator taxa,
Underlined = Coldwater Dependent taxa , Red Shaded are introduced species.
Order
Family
Final Taxa ID
#ofS
% Fof
Beetles
Coleoptera
Dryopidae
Helichus lithophilus
2
7.7
Coleoptera
Dytiscidae
Agabus
4
15.4
Coleoptera
Dytiscidae
Coptotomus longulus
1
3.8
Coleoptera
Dytiscidae
Hydroporus
7
26.9
Coleoptera
Dytiscidae
Laccophilus
1
3.8
Coleoptera
Elmidae
Cleptelmis addenda
2
7.7
Coleoptera
Flmidae
Heterlimnius corpulentus
12
46.2
Coleoptera
Elmidae
Microcylloepus pusillus
1
3.8
Coleoptera
Elmidae
Narpus concolor
3
11.5
Coleoptera
Flmidae
Optioservus sp.
3
11.5
Coleoptera
Flmidae
Optioservus quadrimaculatus
16
61.5
Coleoptera
Elmidae
Ordobrevia nubifera
2
7.7
Coleoptera
Haliplidae
Haliplus
2
7.7
Coleoptera
Haliplidae
Peltodytes
1
3.8
Coleoptera
Hydraenidae
Hydraena
1
3.8
Coleoptera
Hydrophilidae
Hydrobius
7
26.9
Coleoptera
Hydrophilidae
Laccobius
1
3.8
Coleoptera
Hydrophilidae
Paracymus
1
3.8
Coleoptera
Hydrophilidae
Tropisternus lateralis
1
3.8
True Flies
Diptera
Ceratopogonidae
Bezzia/Palpomyia
3
11.5
Diptera
Ceratopogonidae
Ceratopogon
2
7.7
Diptera
Ceratopogonidae
Culicoides
4
15.4
Diptera
Ceratopogonidae
Dasyhelea
1
3.8
Diptera
Ceratopogonidae
Probezzia
2
7.7
Diptera
Chironomidae
Boreochlus persimilus
1
3.8
Diptera
Chironomidae
Brillia
14
53.8
Diptera
Chironomidae
Cardiocladius
5
19.2
Diptera
Chironomidae
Chaetocladius
5
19.2
Diptera
Chironomidae
Corynoneura
3
11.5
Diptera
Chironomidae
Cricotopus
7
26.9
Diptera
Chironomidae
Cricotopus bicinctus Gr.
2
7.7
Diptera
Chironomidae
Cryptochironomus
1
3.8
Diptera
Chironomidae
Diamesa
2
7.7
Diptera
Chironomidae
Dicrotendipes
2
7.7
Diptera
Chironomidae
Diplocladius
1
3JJ
Diptera
Chironomidae
Doithrix
1
3J$
Diptera
Chironomidae
Eukiefferiella
2
7.7
Diptera
Chironomidae
Eukiefferiella Brehmi Gr.
2
H
Diptera
Chironomidae
Eukiefferiella Devonica Gr.
1
3JJ
Diptera
Chironomidae
Eukiefferiella Pseudomontana Gr.
1
3.8
Diptera
Chironomidae
Heleniella
3
11.5
Diptera
Chironomidae
Hydrobaenus
2
7.7
Diptera
Chironomidae
Krenosmittia
2
H
31 March 2008
Aquatic Invertebrate Surveys of BICA Seeps and Sprii
igs
St
Page 15 of 18
Stagliano
Appendix A (cont).
Diptera
Chironomidae
Limnophyes
5
19.2
Diptera
Chironomidae
Macropelopia
4
15.4
Diptera
Chironomidae
Metriocnemus
4
15.4
Diptera
Chironomidae
Micropsectra
15
57.7
Diptera
Chironomidae
Odontomesa
2
7.7
Diptera
Chironomidae
Orthocladius
4
15.4
Diptera
Chironomidae
Pagastia
1
3JJ
Diptera
Chironomidae
Parachironomus
1
3.8
Diptera
Chironomidae
Parakiefferiella
5
19.2
Diptera
Chironomidae
Paralauterborniella nigrohalteris
1
3.8
Diptera
Chironomidae
Parametriocnemus
9
34.6
Diptera
Chironomidae
Paraphaenocladius
3
11.5
Diptera
Chironomidae
Polypedilum
3
11.5
Diptera
Chironomidae
Procladius
2
7.7
Diptera
Chironomidae
Psectrocladius
1
3.8
Diptera
Chironomidae
Pseudochironomus
1
3.8
Diptera
Chironomidae
Pseudodiamesa
4
15.4
Diptera
Chironomidae
Psilometriocnemus
6
23.1
Diptera
Chironomidae
Radotanypus
2
7.7
Diptera
Chironomidae
Tanytarsus
1
3.8
Diptera
Chironomidae
Thienemanniella
4
15.4
Diptera
Chironomidae
Thienemannimyia Gr.
1
3.8
Diptera
Chironomidae
Tvetenia Bavarica Gr.
12
46.2
Diptera
Chironomidae
Tvetenia vitracies Gr.
1
3.8
Diptera
Dixidae
Dixa
6
23.1
Diptera
Dolichopodidae
Dolichopodidae
1
3.8
Diptera
Empididae
Clinocera
3
11.5
Diptera
Empididae
Hemerodromia
3
11.5
Diptera
Psychodidae
Pericoma
1
3.8
Diptera
Ptychopteridae
Ptychoptera
1
3.8
Diptera
Stratiomyidae
Stratiomyia
1
3.8
Diptera
Stratiomyidae
Caloparyphus
7
26.9
Diptera
Stratiomyidae
Euparyphus
6
23.1
Diptera
Tabanidae
Chrysops
2
7.7
Diptera
Tabanidae
Tabanus
1
3.8
Diptera
Tipulidae
Dactylabis
1
3.8
Diptera
Tipulidae
Dicranota
8
30.8
Diptera
Tipulidae
Gonomyia
2
7.7
Diptera
Tipulidae
Hexatoma
1
3.8
Diptera
Tipulidae
Limnophila
1
3.8
Diptera
Tipulidae
Limonia
4
15.4
Diptera
Tipulidae
Limonia (Dicronomyia)
1
3.8
Diptera
Tipulidae
Ormosia
3
11.5
Diptera
Tipulidae
Ormosia (Scleroprocta)
1
3JJ
Diptera
Tipulidae
Tipula
10
38.5
Mayflies
Ephemeroptera
Ameletidae
Ameletus simiilor
1
3JJ
Ephemeroptera
Baetidae
Baetis bicaudatus
1
3JJ
Ephemeroptera
Baetidae
Baetis tricaudatus
16
61.5
Ephemeroptera
Baetidae
Callibaetis ferrugineus
1
3.8
Ephemeroptera
Baetidae
Callibaetis fluctuans
1
3.8
31 March 2008
Aquatic Invertebrate Surveys of BICA Seeps and Springs
Page 16 of 18
Stagliano
Appendix A (cont).
Ephemeroptera
Baetidae
Diphetor hageni
3
11.5
Dragonflies/Damselflies
Odonata
Aeshnidae
Aeshna
1
3.8
Odonata
Aeshnidae
Aeshna umbrosa
1
3.8
Odonata
Coenagrionidae
Argia
2
7.7
Odonata
Coenagrionidae
Amphiagrion abbreviatum
1
3.8
Odonata
Coenagrionidae
Coenagrion/Enallagma
1
3.8
Stoneflies
Plecoptera
Chloroperlidae
Sweltsa
2
7.7
Plecoptera
Chloroperlidae
Paraperla cf. frontalis
1
3JJ
Plecoptera
Nemouridae
Amphinemura banksi
16
61.5
Plecoptera
Nemouridae
Malenka
6
23.1
Plecoptera
Nemouridae
Zapada oregonensis
1
3JJ
Plecoptera
Perlidae
Hesperoperla pacifica
13
50.0
Plecoptera
Perlodidae
Perlodidae
1
3.8
Caddis/lies
Trichoptera
Hydropsychidae
Hydropsyche californica
2
7.7
Trichoptera
Hydropsychidae
Hydropsyche confusa
6
23.1
Trichoptera
Hydropsychidae
Hydropsyche morosa gr.
3
11.5
Trichoptera
Hydroptilidae
Ochrotrichia
6
23.1
Trichoptera
Hydroptilidae
Hydroptila
1
3.8
Trichoptera
Lepidostomatidae
Lepidostoma
2
7.7
Trichoptera
Lepidostomatidae
Lepidostoma pluviale
3
11.5
Trichoptera
Lepidostomatidae
Lepidostoma unicolor
12
46.2
Trichoptera
Limnephilidae
Hesperophylax designatus
6
23.1
Trichoptera
Limnephilidae
Homophylax
1
3JJ
Trichoptera
Limnephilidae
Limnephilus
5
19.2
Trichoptera
Limnephilidae
Nemotaulius hostilis
1
3.8
Trichoptera
Philopotamidae
Dolophilodes
1
3.8
Trichoptera
Rhyacophilidae
Rhyacophila Brunnea Gr.
3
11.5
Trichoptera
Rhyacophilidae
Rhyacophila oreta
3
11.5
Trichoptera
Rhyacophilidae
Rhyacophila rotunda
2
12
Trichoptera
Rhyacophilidae
Rhyacophila verrula
2
12
Trichoptera
Uenoidae
Neothremma alicia
2
12
Peaclams
Veneroida
Pisidiidae
Sphaerium
4
15.4
Veneroida
Pisidiidae
Pisidium casertanum
1
3.8
Snails
B asommatophor a
Lymnaeidae
Fossaria humilis
4
15.4
Basommatophora
Lymnaeidae
Fossaria obrussa
2
7.7
B asommatophor a
Lymnaeidae
Lymnaea stagnalis
1
3.8
Basommatophora Lymnaeidae Pseudosuccinea columella 3 11.5
B asommatophor a
Physidae
Physella
19
73.1
Basommatophora
Physidae
Physella zionensis
1
3.8
Heterostropha
Planorbidae
Planorbula campestris
3
11.5
Heterostropha
Valvatidae
Valvata sincera
5
19.2
Heterostropha
Valvatidae
Valvata lewisi
9
34.6
Non-Insect Oligochaeta Worms 1 Flatworms
Turbellaria
Polycelis coronata
4
15.4
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Stagliano
Appendix A (cont).
Turbellaria
Nematoda
Haplotaxida
Haplotaxida
Lumbriculida
Crustacea
Lumbricidae
Tubificidae
Lumbriculidae
Turbellaria
Nematoda
Lumbricina
Tubificidae
Lumbriculidae
1
3.8
2
7.7
1
3.8
1
3.8
2
7.7
Ostracoda
Mites
Trombidiformes
Trombidiformes
Trombidiformes
Hygrobatidae
Hygrobatidae
Limnocharidae
Ostracoda
Tyrellia
Hygrobates
Rhyncholimnochares
15.4
1
3.8
1
3.8
1
3.8
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Aquatic Invertebrate Surveys of BICA Seeps and Springs
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Stagliano